22 results · 14ms · Sources: EU EUDAMED, US FDA

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Cystonephroscope-endoscopic diagnosis and treatment within the bladder, urethra, and kidney Model Numbers: CYF-5, CYF-VH, CYF-VHR.

FDA Recall
Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code FAJ·September 25, 2023

Model No. CYF-5, Cystonephrofiberscope

FDA Recall
Open, Classified ·Shirakawa Olympus Co., Ltd. Azaokamiyama 3-1 Oazaodakura; Nishigo-Mura Nishishirakawa-Gun Japan·Product code FAJ·December 4, 2023

Model No. CYF-5R, Cystonephrofiberscope

FDA Recall
Open, Classified ·Shirakawa Olympus Co., Ltd. Azaokamiyama 3-1 Oazaodakura; Nishigo-Mura Nishishirakawa-Gun Japan·Product code FAJ·December 4, 2023

Olympus CYSTONEPHROFIBERSCOPE Model: CYF-5

FDA Recall
Open, Classified ·Olympus Corporation of the Americas·Product code FAJ·April 20, 2022

Model No. CYF-VHR, CYSTO-NEPHRO VIDEOSCOPE

FDA Recall
Open, Classified ·Shirakawa Olympus Co., Ltd. Azaokamiyama 3-1 Oazaodakura; Nishigo-Mura Nishishirakawa-Gun Japan·Product code FAJ·December 4, 2023

Model No. CYF-VH, CYSTO-NEPHRO VIDEOSCOPE

FDA Recall
Open, Classified ·Shirakawa Olympus Co., Ltd. Azaokamiyama 3-1 Oazaodakura; Nishigo-Mura Nishishirakawa-Gun Japan·Product code FAJ·December 4, 2023

Model No. CYF-V2, VISERA Cysto-Nephro Videoscope

FDA Recall
Open, Classified ·Shirakawa Olympus Co., Ltd. Azaokamiyama 3-1 Oazaodakura; Nishigo-Mura Nishishirakawa-Gun Japan·Product code FAJ·December 4, 2023

Model No. CYF-V2R, VISERA Cysto-Nephro Videoscope

FDA Recall
Open, Classified ·Shirakawa Olympus Co., Ltd. Azaokamiyama 3-1 Oazaodakura; Nishigo-Mura Nishishirakawa-Gun Japan·Product code FAJ·December 4, 2023

ADVANTA VXT, 4-7X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

ADVANTA VXT, 5-8X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

ADVANTA VXT, 5X40, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

ADVANTA VXT, 4-7X45, 2GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

ADVANTA VXT, 5X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

ADVANTA VXT, 4-7X70, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

ADVANTA VXT, 5-8X80, 1GDS, FH, TPR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

ADVANTA VXT, 5X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

ADVANTA VXT, 4-6X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

ADVANTA VXT, 4-7X80, 1GDS, FH, TPR-TW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

ADVANTA VXT, 5X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

ADVANTA VXT, 4-7X45, 1GDS, CH, TPR-SW. Single-Ended Slider GDS. Vascular graft

FDA Recall
Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024